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5,8-Dihydroxy-1,4-Naphthoquinone

    • Product Name 5,8-Dihydroxy-1,4-Naphthoquinone
    • Alias Lawsone
    • Einecs 202-264-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    273793

    Chemical Name 5,8-Dihydroxy-1,4-Naphthoquinone
    Molecular Formula C10H6O4
    Molar Mass 190.15 g/mol
    Appearance Yellow to orange crystalline powder
    Melting Point 264-266 °C
    Boiling Point Decomposes
    Solubility In Water Slightly soluble
    Cas Number 82-86-0
    Structure Naphthoquinone core with hydroxyl groups at positions 5 and 8
    Synonyms Juglone
    Pubchem Cid 10216
    Density 1.581 g/cm³

    As an accredited 5,8-Dihydroxy-1,4-Naphthoquinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5,8-Dihydroxy-1,4-Naphthoquinone (10g) is packaged in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 5,8-Dihydroxy-1,4-naphthoquinone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Standard packaging meets regulatory requirements for chemical transport. The chemical is labeled with proper hazard and handling information, ensuring safe transit by ground or air according to local and international shipping regulations (e.g., DOT, IATA, IMDG).
    Storage 5,8-Dihydroxy-1,4-naphthoquinone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature or as indicated on the supplier’s label. Avoid excessive heat and sources of ignition to maintain stability and prevent decomposition.
    Application of 5,8-Dihydroxy-1,4-Naphthoquinone

    Applications of 5,8-Dihydroxy-1,4-Naphthoquinone in Industrial Manufacturing

    As a specialty manufacturer of 5,8-Dihydroxy-1,4-Naphthoquinone (commonly known as Lawsone), we support industrial customers across several established sectors requiring high-purity intermediate chemicals. Below, we detail the principal downstream use cases, specifying precise industry standards, functional dosage guidelines, integration within manufacturing sequences, and the final product formats produced by our clients.

    1. Hair Dye Ingredient Production

    Hair color formulators in the cosmetics sector rely on this quinone exclusively for the synthesis of natural-origin and permanent hair dyes, leveraging its molecular affinity for keratin and direct dyeing capability. Precise control of concentration allows tailored color intensity and stability during blending with oxidants or other dye precursors. Manufacturers optimize dye shade and fastness through managed pH and selection of compatible coupling agents in batch or continuous processes that demand careful quality monitoring. The resulting finished goods occupy premium and natural hair treatment markets worldwide.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • U.S. FDA 21 CFR Part 73.2190 (Hair Dye Exempt Color Additives)
    • ISO 21148 (Cosmetics — Microbiology)
    • Cosmetic Ingredient Review (CIR) Safety Assessments

    Typical usage ratio

    • 0.02% – 2% by weight, adjusted according to the base shade, depth, and target color saturation

    Downstream process integration

    • Dissolved during the pigment compounding and dye precursor phase prior to emulsification and pH adjustment

    Final product types

    • Permanent and semi-permanent hair color creams
    • Henna-based hair dye formulations
    • Liquid dye concentrates for salon and home use

    2. Biologically-Derived Textile Dye Manufacture

    Textile dyeing plants incorporate the compound as a core coloring agent for eco-friendly cellulosic and protein fiber dyeing systems, selecting it for its strong affinity with cotton, wool, and silk substrates. Dosage precision aligns chroma uniformity and wash fastness, while compliance testing assures safe residual limits on finished fabrics. Dyeing occurs in jet, pad-batch, or exhaust systems during the wet processing sequences; color adjustment is achieved through modifiers and controlled reaction times under regulated thermal conditions. Licit downstream imports often demand transparent traceability and certification.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • REACH Regulation (EC) No 1907/2006 (Annex XVII dyes)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 105 series (Textiles — Fastness Testing)

    Typical usage ratio

    • 0.1% – 1.5% on fiber weight, depending on fiber type and target depth of shade

    Downstream process integration

    • Introduced into dye bath during initial wetting or simultaneously with mordants in preliquor additions; followed by fixation and post-wash neutralization

    Final product types

    • Dyed cotton yarns and woven fabrics
    • Regenerative cellulose textiles (viscose, lyocell)
    • Silk and wool garments with natural color bases

    3. Pharmaceutical Intermediate for Vitamin K Synthesis

    This naphthoquinone serves as a validated chemical synthon in regulated Active Pharmaceutical Ingredient (API) manufacturing, particularly for menadione (vitamin K3) and related analogues. API manufacturers use it in sequence-specific steps that involve selective reduction, methylation, or condensation reactions, often within GMP-certified environments. Dialed production purity minimizes side-reactions and meets pharmacopoeial specifications for downstream drug or supplement formulation.

    Industry compliance standards

    • US Pharmacopeia (USP) regulations for Vitamin K substances
    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • Health Canada GMP Guidelines (GUI-0001)

    Typical usage ratio

    • Proportional to desired batch yield; generally 1 molar equivalent as an intermediate, followed by full conversion to active vitamin K derivatives

    Downstream process integration

    • Charged into the reaction vessel after precursor assembly, utilized during condensation, methylation, or reduction—prior to crystallization and purification steps

    Final product types

    • Menadione (Vitamin K3) for feed and pharmaceutical use
    • Vitamin K analog intermediates for further functionalization
    • Finished pharmaceutical ingredients for oral formulations

    4. Organic Electronic Materials & Conductive Pigment Formulation

    Advanced manufacturers leverage the electron-accepting properties of this compound in formulating conductive polymers, printable electronic inks, and as a functional pigment in organic electronic components. The raw material delivers controlled charge transport and color performance in flexible thin-film applications, requiring careful blending with carriers and stabilizers. Use concentrations vary by substrate compatibility and device design, and industrial quality checks validate batch-to-batch consistency, alignment with purity specifications, and electrochemical stability suitable for downstream assembly.

    Industry compliance standards

    • RoHS 2011/65/EU (Restriction of Hazardous Substances in electronics)
    • IEC 61249-2-21 standards for halogen-free materials
    • IPC-4101B (Requirements for Base Materials for Rigid and Multilayer Printed Boards)
    • IEC 60068 (Environmental Testing of Electronic Equipment)

    Typical usage ratio

    • 0.1% – 0.5% by dry weight for ink or polymer formulations; ratios tuned according to targeted conductivity and color depth requirements

    Downstream process integration

    • Dispersed with solvent carriers and other functional additives during the pigment dispersion or ink mixing phase; homogenized prior to screen printing or thin film casting

    Final product types

    • Conductive pastes and inks for printed circuit boards
    • Organic TFT (thin film transistor) layers
    • Colored conductive polymer coatings for flexible electronics

    5. Analytical Reagents for Metal Detection and Research

    Laboratory and industrial reagent producers use the compound as a chromogenic agent in complexometric titration kits, and as a precursor for specialty detection reagents in analytical chemistry. Its selective chelating properties enable colorimetric assays for various metal ions in environmental, food, and industrial water testing. Production processes require stringent QC and validation against reference materials to ensure diagnostic reliability and repeatable quantification thresholds. Variability in formulation reflects the metal specificity and sensitivity required for each assay.

    Industry compliance standards

    • ISO 17025 (Testing and Calibration Laboratories)
    • ASTM D1687 (Colorimetric Determination in Water Testing)
    • Food Chemicals Codex (FCC) for analytical reagents
    • Quality control documentation per GLP (Good Laboratory Practice)

    Typical usage ratio

    • 1 – 200 mg/L in reagent formulations depending on test kit design and target detection limit for specific metal ions

    Downstream process integration

    • Incorporated as a reactant or indicator in the preparation of complexometric or colorimetric test kits; mixed during batch reagent preparation under controlled environmental conditions

    Final product types

    • Colorimetric metal detection kits for water analysis
    • Analytical standards for laboratory chemistry use
    • Research-grade reagents for academic and industrial R&D
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    Competitive 5,8-Dihydroxy-1,4-Naphthoquinone prices that fit your budget—flexible terms and customized quotes for every order.

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